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一例具有不寻常临床病程的复发性右侧心脏平滑肌肉瘤的多模态成像。

Multimodality imaging of a recurrent case of right-sided cardiac leiomyosarcoma with an unusual clinical course.

作者信息

Astarcıoğlu Mehmet Ali, Kalçık Macit, Gürsoy Mustafa Ozan, Gündüz Sabahattin, Özkan Mehmet

机构信息

Department of Cardiology, Kartal Koşuyolu Heart Training and Research Hospital, İstanbul, Turkey.

出版信息

Turk Kardiyol Dern Ars. 2015 Jun;43(4):372-5. doi: 10.5543/tkda.2015.09125.

Abstract

Primary cardiac sarcoma is an uncommon entity and is related with poor long-term survival. Presented here is an unusual case of right atrial leiomyosarcoma which almost completely occluded both the right atrium and ventricle and destroyed the tricuspid valve. Multimodality imaging was used to characterize the mass and guide surgical management. A combination of two radical surgical excisions and both radiation and chemotherapy resulted in a better long-term outcome. The patient was one of the longest survivors.

摘要

原发性心脏肉瘤是一种罕见的疾病,与长期生存率低相关。本文介绍了一例不寻常的右心房平滑肌肉瘤病例,该肿瘤几乎完全阻塞了右心房和右心室,并破坏了三尖瓣。采用多模态成像对肿块进行特征描述并指导手术治疗。两次根治性手术切除以及放疗和化疗相结合,带来了更好的长期预后。该患者是存活时间最长的患者之一。

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